{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Komorniki",
      "state": "N/A",
      "country": "Poland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86065",
      "recalling_firm": "ARJOHUNTLEIGH POLSKA Sp. z.o.o.",
      "address_1": "Ui. Ks. Piotra Wawrzyniaka 2",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide) to states of:: FL, KS, LA and countries of:: Australia, Brazil, Canada, France and Germany.",
      "recall_number": "Z-2821-2020",
      "product_description": "Bariatric Bed Frame System    The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments. It is not intended for use in the home care environment.",
      "product_quantity": "145 units",
      "reason_for_recall": "Modular Junction Box (MJB) cables can melt and affect the bed functionality.",
      "recall_initiation_date": "20200721",
      "center_classification_date": "20200818",
      "termination_date": "20210217",
      "report_date": "20200826",
      "code_info": "Serial number range: P0597830  to P0610470  Model numbers:  FXX21A4A4AKFBB, FXX21A4D3AMFBA, FXX21C4B1AAABB, FXX21C4B4ABQBA, FXX21A4C4ACGBB, FXX21A4A1ABUBA, FXX21A6C2ABPBB, FXX21C4B1AAABA, FX811B3B4AMABB, FXX21C4D4AKBBB, FX611A2B2ALVBB"
    }
  ]
}